BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    STEAM DOT BLU PROCESS INDICATOR

    K Number: K111453 · Decision Apr 5, 2012
    View on FDA
    Classifications
    1
    FEI Numbers
    130
    Registration Numbers
    130
    Same Product Code
    264
    Applicant Total
    25
    Review Days
    316

    Research this 510(k) in seconds

    The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Device Name
    STEAM DOT BLU PROCESS INDICATOR
    K Number
    K111453
    Device Class
    FDA class 2
    Clearance Type
    Abbreviated
    Regulation Number
    880.2800
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Propper Mfg. Co., Inc.
    Date Received
    May 25, 2011
    Decision Date
    April 5, 2012
    Product Code
    JOJ
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    JOJ Indicator, Physical/Chemical Sterilization Process

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (JOJ), ordered by most recent decision date.

    LF Process Indicator Tape for Steam Sterilization

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SafeSecure Steam Sterilization Process Indicator (4012, 4013, 4014, 4016); SafeSecure Vaporized Hydrogen Peroxide Sterilization Process Indicator (4211, 4212, 4213)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DISINTEK™ PA Test Strips

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Rapicide PA High-Level Disinfection Test Strip Model Ref # = ML02-0118

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VERIFY STEAM Integrating Indicator

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Green Card Bowie-Dick Test (BD115)

    FDA 510(k)
    FDA Class 2 ·General Hospital
    View all

    Other Clearances by Propper Mfg. Co., Inc.

    K Number Device Name
    K102894 CLASSIX CHEMICAL STERILIZATION INDICATOR
    K082620 ONCE-A-DAY VERTOS TEST PACK
    K031152 PROPPER VAPOR LINE PCD (STEAM STERILIZATION PROCESS CHALLENGE TEST)
    K991618 BI-O.K. SELF-CONTAINED BIOLOGICAL INDICATOR
    K991276 PASS/FAIL CHALLENGE PACK
    K973585 PROPPER EO LINE ETHYLENE OXIDE STERILIZATION INTEGRATOR
    K972747 BI-O.K. EO GAS BIOLOGICAL TEST-PAK (269305,269310,269320)
    K961156 ONCE-A-DAY BOWIE AND DICK TEST PACK.
    K921798 PROPPER SUPER SERACULT(R)
    K915804 PROPPER LARYNGOSCOPE BLADES W FIBER OPTIC ILLUM.
    Search all 25 clearances from Propper Mfg. Co., Inc. →